-
1
-
-
0033066357
-
Synthesis of podophyllotoxin and related analogues: Part X - Tetralone esters as intermediates for synthesis of analogues of β-apopicropodophyllin
-
Anjanamurthy C., Basavaraju Y.B. Synthesis of podophyllotoxin and related analogues: part X - tetralone esters as intermediates for synthesis of analogues of β-apopicropodophyllin. Ind. J. Chem. B 38:1999;137-140
-
(1999)
Ind. J. Chem.
, vol.38
, pp. 137-140
-
-
Anjanamurthy, C.1
Basavaraju, Y.B.2
-
2
-
-
0034434229
-
Design of two etoposide-amsacrine conjugates: Topoisomerase II and tubuline polymerization inhibition and relation to cytotoxicity
-
Arimondo P., Boukarim C., Bailly C., Dauzonne D., Monneret C. Design of two etoposide-amsacrine conjugates: topoisomerase II and tubuline polymerization inhibition and relation to cytotoxicity. Anticancer Drug Des. 15:2000;413-421
-
(2000)
Anticancer Drug Des.
, vol.15
, pp. 413-421
-
-
Arimondo, P.1
Boukarim, C.2
Bailly, C.3
Dauzonne, D.4
Monneret, C.5
-
4
-
-
0036244606
-
F 11782, a novel catalytic inhibitor of topoisomerases I and II, induces atypical, yet cytotoxic DNA double-strand breaks in CHO-K1 cells
-
Barret J.M., Etievant C., Baudouin C., Skov K., Charveron M., Hill B.T. F 11782, a novel catalytic inhibitor of topoisomerases I and II, induces atypical, yet cytotoxic DNA double-strand breaks in CHO-K1 cells. Anticancer Res. 22:2002;187-192
-
(2002)
Anticancer Res.
, vol.22
, pp. 187-192
-
-
Barret, J.M.1
Etievant, C.2
Baudouin, C.3
Skov, K.4
Charveron, M.5
Hill, B.T.6
-
5
-
-
0036110357
-
Synthesis of analogues of podophyllotoxin: Tetralones as intermediates for the synthesis of analogues of apopicropodophyllin
-
Basavaraju Y.B., Devaraju Y. Synthesis of analogues of podophyllotoxin: tetralones as intermediates for the synthesis of analogues of apopicropodophyllin. Ind. J. Heterocyclic Chem. 11:2002;229-232
-
(2002)
Ind. J. Heterocyclic Chem.
, vol.11
, pp. 229-232
-
-
Basavaraju, Y.B.1
Devaraju, Y.2
-
6
-
-
0032985328
-
New podophyllotoxin derivatives as potential anticancer agents: Synthesis and cytotoxicity of 4(O-propenylpodophyllotoxin ethers
-
Bathini Y., Scholte A., Kelly S., Micetich R.G., Daneshtalab M. New podophyllotoxin derivatives as potential anticancer agents: synthesis and cytotoxicity of 4(O-propenylpodophyllotoxin ethers. Synth. Commun. 29:1999;379-385
-
(1999)
Synth. Commun.
, vol.29
, pp. 379-385
-
-
Bathini, Y.1
Scholte, A.2
Kelly, S.3
Micetich, R.G.4
Daneshtalab, M.5
-
7
-
-
2342666669
-
Bioprospecting for podophyllotoxin
-
J. Janick, & A. Whipkey. Alexandria: ASHS Press
-
Bedir E., Khan I., Moraes R.M. Bioprospecting for podophyllotoxin. Janick J., Whipkey A. Trends in New Crops and New Uses. 2002;545-549 ASHS Press, Alexandria
-
(2002)
Trends in New Crops and New Uses
, pp. 545-549
-
-
Bedir, E.1
Khan, I.2
Moraes, R.M.3
-
8
-
-
0020406202
-
An investigation of the antiviral activity of Podophyllum peltatum
-
Bedows E., Hatfield G.M. An investigation of the antiviral activity of Podophyllum peltatum. J. Nat. Prod. 45:1982;725-729
-
(1982)
J. Nat. Prod.
, vol.45
, pp. 725-729
-
-
Bedows, E.1
Hatfield, G.M.2
-
9
-
-
0021271378
-
Antineoplastic and antiherpetic activity of spermidine catecholamide iron chelators
-
Bergeron R.J., Cavanaugh P.F. Jr., Kline S.J., Hugues R.G., Elliot G.T., Porter C.W. Antineoplastic and antiherpetic activity of spermidine catecholamide iron chelators. Biochem. Biophys. Res. Commun. 121:1984;848-854
-
(1984)
Biochem. Biophys. Res. Commun.
, vol.121
, pp. 848-854
-
-
Bergeron, R.J.1
Cavanaugh Jr., P.F.2
Kline, S.J.3
Hugues, R.G.4
Elliot, G.T.5
Porter, C.W.6
-
10
-
-
0033399646
-
Hydrolytic enzymatic transformation of advanced synthetic intermediates: On the choice of the organic cosolvent
-
Berkowitz D.B., Hartung R.E., Choi S. Hydrolytic enzymatic transformation of advanced synthetic intermediates: on the choice of the organic cosolvent. Tetrahedron: Asymmetry. 10:1999;4513-4520
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 4513-4520
-
-
Berkowitz, D.B.1
Hartung, R.E.2
Choi, S.3
-
11
-
-
0033960568
-
Enzyme-assisted asymmetric total synthesis of (-)-podophyllotoxin and (-)-picropodophyllin
-
Berkowitz D.B., Choi S., Maeng J.H. Enzyme-assisted asymmetric total synthesis of (-)-podophyllotoxin and (-)-picropodophyllin. J. Org. Chem. 65:2000;847-860
-
(2000)
J. Org. Chem.
, vol.65
, pp. 847-860
-
-
Berkowitz, D.B.1
Choi, S.2
Maeng, J.H.3
-
12
-
-
0034689853
-
Novel reverse Kahne-type glycosylation: Access to O-, N-, and C-linked epipodophyllotoxin conjugates
-
Berkowitz D.B., Choi S.J., Bhuniya D., Shoemaker R.K. Novel reverse Kahne-type glycosylation: access to O-, N-, and C-linked epipodophyllotoxin conjugates. Org. Lett. 2:2000;1149-1152
-
(2000)
Org. Lett.
, vol.2
, pp. 1149-1152
-
-
Berkowitz, D.B.1
Choi, S.J.2
Bhuniya, D.3
Shoemaker, R.K.4
-
13
-
-
0029704454
-
Podophyllotoxin in the treatment of genital warts
-
Beutner K.R. Podophyllotoxin in the treatment of genital warts. Curr. Probl. Dermatol. 24:1996;227-232
-
(1996)
Curr. Probl. Dermatol.
, vol.24
, pp. 227-232
-
-
Beutner, K.R.1
-
14
-
-
0034741843
-
Aryltetralin Lignans: Chemistry, Pharmacology and Biotransformations
-
Botta B., Delle Monache G., Misiti D., Vitali A., Zappia G. Aryltetralin Lignans: Chemistry, Pharmacology and Biotransformations. Curr. Med. Chem. 8:2001;1363-1381
-
(2001)
Curr. Med. Chem.
, vol.8
, pp. 1363-1381
-
-
Botta, B.1
Delle Monache, G.2
Misiti, D.3
Vitali, A.4
Zappia, G.5
-
15
-
-
0000842931
-
Matairesinol as precursor of Podophyllum lignans
-
Bromhead A.J., Rahman M.M., Dewick P.M., Jackson D.E., Lucas J.A. Matairesinol as precursor of Podophyllum lignans. Phytochemistry. 30:1991;1489-1492
-
(1991)
Phytochemistry
, vol.30
, pp. 1489-1492
-
-
Bromhead, A.J.1
Rahman, M.M.2
Dewick, P.M.3
Jackson, D.E.4
Lucas, J.A.5
-
16
-
-
0034640721
-
Modified CoMFA methods for the analysis of antineoplastic effects of lignan analogues
-
Broughton H.B., Gordaliza M., Castro M.A., Miguel del Corral J.M., San Feliciano A. Modified CoMFA methods for the analysis of antineoplastic effects of lignan analogues. J. Mol. Struct. (TheoChem). 504:2000;287-294
-
(2000)
J. Mol. Struct. (TheoChem)
, vol.504
, pp. 287-294
-
-
Broughton, H.B.1
Gordaliza, M.2
Castro, M.A.3
Miguel Del Corral, J.M.4
San Feliciano, A.5
-
19
-
-
0035098846
-
High yield of podophyllotoxin from leaves of Podophyllum peltatum by in situ conversion of podophyllotoxin 4-O-β-D-glucopyranoside
-
Canel C., Dayan F.E., Ganzera M., Khan I.A., Rimando A., Burandt C.L., Moraes R.M. High yield of podophyllotoxin from leaves of Podophyllum peltatum by in situ conversion of podophyllotoxin 4-O-β-D-glucopyranoside. Planta Med. 67:2001;97-99
-
(2001)
Planta Med.
, vol.67
, pp. 97-99
-
-
Canel, C.1
Dayan, F.E.2
Ganzera, M.3
Khan, I.A.4
Rimando, A.5
Burandt, C.L.6
Moraes, R.M.7
-
20
-
-
0034918788
-
Antitumor agents: Synthesis and biological evaluation of new compounds related to podophyllotoxin, containing the 2,3-dihydro-1,4-benzodioxin system
-
Capilla A.S., Sanchez I., Caignard D.H., Renard P., Pujol M.D. Antitumor agents: synthesis and biological evaluation of new compounds related to podophyllotoxin, containing the 2,3-dihydro-1,4-benzodioxin system. Eur. J. Med. Chem. 36:2001;389-393
-
(2001)
Eur. J. Med. Chem.
, vol.36
, pp. 389-393
-
-
Capilla, A.S.1
Sanchez, I.2
Caignard, D.H.3
Renard, P.4
Pujol, M.D.5
-
23
-
-
0037366453
-
Síntesis and cytotoxicity of podophyllotoxin analogues modified in the A-ring
-
Castro M.A., Miguel del Corral J.M., Gordaliza M., Grande C., Gómez-Zurita M.A., García-Grávalos M.D., San Feliciano A. Síntesis and cytotoxicity of podophyllotoxin analogues modified in the A-ring. Eur. J. Med. Chem. 38:2003;65-74
-
(2003)
Eur. J. Med. Chem.
, vol.38
, pp. 65-74
-
-
Castro, M.A.1
Miguel Del Corral, J.M.2
Gordaliza, M.3
Grande, C.4
Gómez-Zurita, M.A.5
García-Grávalos, M.D.6
San Feliciano, A.7
-
24
-
-
0142188555
-
Synthesis, cytotoxicity and antiviral activity of podophyllotoxin analogues modified in the E-ring
-
Castro M.A., Miguel del Corral J.M., Gordaliza M., Gómez-Zurita M.A., De la Puente M.L., Betancur-Galvis L.A., Sierra J., García- Grávalos M.D., San Feliciano A. Synthesis, cytotoxicity and antiviral activity of podophyllotoxin analogues modified in the E-ring. Eur. J. Med. Chem. 38:2003;899-911
-
(2003)
Eur. J. Med. Chem.
, vol.38
, pp. 899-911
-
-
Castro, M.A.1
Miguel Del Corral, J.M.2
Gordaliza, M.3
Gómez-Zurita, M.A.4
De La Puente, M.L.5
Betancur-Galvis, L.A.6
Sierra, J.7
García-Grávalos, M.D.8
San Feliciano, A.9
-
25
-
-
0036644246
-
Pd-catalyzed route to (+/-)-podophyllotoxin skeleton. Synthesis of the aryltetralin derivative
-
Charruault L., Michelet V., Genet J.P. Pd-catalyzed route to (+/-)-podophyllotoxin skeleton. Synthesis of the aryltetralin derivative. Tetrahedron Lett. 43:2002;4757-4760
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 4757-4760
-
-
Charruault, L.1
Michelet, V.2
Genet, J.P.3
-
26
-
-
0035690314
-
Development of suspension culture of Podophyllum hexandrum for production of podophyllotoxin
-
Chattopadhyay S., Srivastava A.K., Bhojwani S.S., Bisaria V.S. Development of suspension culture of Podophyllum hexandrum for production of podophyllotoxin. Biotechnol. Lett. 23:2001;2063-2066
-
(2001)
Biotechnol. Lett.
, vol.23
, pp. 2063-2066
-
-
Chattopadhyay, S.1
Srivastava, A.K.2
Bhojwani, S.S.3
Bisaria, V.S.4
-
27
-
-
0036207003
-
Production of podophyllotoxin by plant cell cultures of Podophyllum hexandrum in bioreactor
-
Chattopadhyay S., Srivastava A.K., Bhojwani S.S., Bisaria V.S. Production of podophyllotoxin by plant cell cultures of Podophyllum hexandrum in bioreactor. J. Biosci. Bioeng. 93:2002;215-220
-
(2002)
J. Biosci. Bioeng.
, vol.93
, pp. 215-220
-
-
Chattopadhyay, S.1
Srivastava, A.K.2
Bhojwani, S.S.3
Bisaria, V.S.4
-
28
-
-
0842305665
-
Optimization of culture parameters for production of podophyllotoxin in suspension culture of Podophyllum hexandrum
-
Chattopadhyay S., Srivastava A.K., Bisaria V.S. Optimization of culture parameters for production of podophyllotoxin in suspension culture of Podophyllum hexandrum. Appl. Microbiol. Biotechnol. 102:2002;381-393
-
(2002)
Appl. Microbiol. Biotechnol.
, vol.102
, pp. 381-393
-
-
Chattopadhyay, S.1
Srivastava, A.K.2
Bisaria, V.S.3
-
29
-
-
0037255507
-
Effect of major nutrients on podophyllotoxin production in Podophyllum hexandrum suspension cultures
-
Chattopadhyay S., Mehra R.S., Srivastava A.K., Bhojwani S.S., Bisaria V.S. Effect of major nutrients on podophyllotoxin production in Podophyllum hexandrum suspension cultures. Appl. Microbiol. Biotechnol. 60:2003;541-546
-
(2003)
Appl. Microbiol. Biotechnol.
, vol.60
, pp. 541-546
-
-
Chattopadhyay, S.1
Mehra, R.S.2
Srivastava, A.K.3
Bhojwani, S.S.4
Bisaria, V.S.5
-
30
-
-
0034634366
-
The interaction of the B-ring of colchicine with α-tubulin: A novel footprinting approach
-
Chaudhuri A.R., Seetharamalu P., Schwarz P.M., Hausheer F.H., Luduena R.F. The interaction of the B-ring of colchicine with α-tubulin: a novel footprinting approach. J. Mol. Biol. 303:2000;679-692
-
(2000)
J. Mol. Biol.
, vol.303
, pp. 679-692
-
-
Chaudhuri, A.R.1
Seetharamalu, P.2
Schwarz, P.M.3
Hausheer, F.H.4
Luduena, R.F.5
-
31
-
-
0346355490
-
Two new methods for synthesis of 4 β-amino-4-deoxypodophyllotoxin and 4 β-amino-4′-demethyl-4-deoxypodophyllotoxin
-
Chen S.Y., Yu Y.P., You J.Z., Chen Y.Z. Two new methods for synthesis of 4 β-amino-4-deoxypodophyllotoxin and 4 β-amino-4′-demethyl-4- deoxypodophyllotoxin. Chem. J. Chin. Univ. 21:2000;1064-1066
-
(2000)
Chem. J. Chin. Univ.
, vol.21
, pp. 1064-1066
-
-
Chen, S.Y.1
Yu, Y.P.2
You, J.Z.3
Chen, Y.Z.4
-
32
-
-
0028208869
-
New metabolites, tetrahydrofuran lignans, produced by Streptomyces sp. IT-44
-
Chiung Y.M., Hayashi H., Matsumoto H., Otani T., Yoshida K., Huang M.Y., Chen R.X., Liu J.R., Nakayama M. New metabolites, tetrahydrofuran lignans, produced by Streptomyces sp. IT-44. J. Antibiot. 47:1994;487-491
-
(1994)
J. Antibiot.
, vol.47
, pp. 487-491
-
-
Chiung, Y.M.1
Hayashi, H.2
Matsumoto, H.3
Otani, T.4
Yoshida, K.5
Huang, M.Y.6
Chen, R.X.7
Liu, J.R.8
Nakayama, M.9
-
33
-
-
0000734820
-
Antitumor agents 164, podophenazine, 2″,3″- dichloropodophenazine, benzopodophenazine, and their 4 β-p-nitroaniline derivatives as novel DNA topoisomerase II inhibitors
-
Cho S.J., Kashiwada Y., Bastow K.F., Cheng Y.C., Lee K.H. Antitumor agents 164, podophenazine, 2″,3″-dichloropodophenazine, benzopodophenazine, and their 4 β-p-nitroaniline derivatives as novel DNA topoisomerase II inhibitors. J. Med. Chem. 39:1996;1396-1402
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1396-1402
-
-
Cho, S.J.1
Kashiwada, Y.2
Bastow, K.F.3
Cheng, Y.C.4
Lee, K.H.5
-
34
-
-
0029798194
-
Topical treatment of venereal warts: A comparative open study of podophyllotoxin cream versus solution
-
Claesson U., Lassus A., Happonen H., Hostrom L., Siboulet A. Topical treatment of venereal warts: a comparative open study of podophyllotoxin cream versus solution. Int. J. STD AIDS. 7:1996;429-434
-
(1996)
Int. J. STD AIDS
, vol.7
, pp. 429-434
-
-
Claesson, U.1
Lassus, A.2
Happonen, H.3
Hostrom, L.4
Siboulet, A.5
-
35
-
-
0141516298
-
Dearomatizing cyclization of arylsufonylalkoxymethyl lithiums: A route to the podophyllotoxin skeleton
-
Clayden J., Kenworthy M.N., Helliwell M. Dearomatizing cyclization of arylsufonylalkoxymethyl lithiums: a route to the podophyllotoxin skeleton. Org. Lett. 5:2003;831-834
-
(2003)
Org. Lett.
, vol.5
, pp. 831-834
-
-
Clayden, J.1
Kenworthy, M.N.2
Helliwell, M.3
-
36
-
-
0000951786
-
Conformational analysis of synthetic neolignans active against leishmaniasis, using the molecular mechanics method (MM2)
-
Costa M.C.A., Takahata Y. Conformational analysis of synthetic neolignans active against leishmaniasis, using the molecular mechanics method (MM2). J. Comput. Chem. 18:1997;712-721
-
(1997)
J. Comput. Chem.
, vol.18
, pp. 712-721
-
-
Costa, M.C.A.1
Takahata, Y.2
-
37
-
-
0033862933
-
First synthesis and pharmacological evaluation of benzoindolizidine and benzoquinolizidine analogues of α- And β-peltatin
-
Couture S.O. First synthesis and pharmacological evaluation of benzoindolizidine and benzoquinolizidine analogues of α- and β-peltatin. Bioorg. Med. Chem. 8:2000;2113-2125
-
(2000)
Bioorg. Med. Chem.
, vol.8
, pp. 2113-2125
-
-
Couture, S.O.1
-
38
-
-
0036796823
-
Meiotic telomere clustering is inhibited by colchicine but does not require cytoplasmic microtubules
-
Cowan C.R., Cande W.Z. Meiotic telomere clustering is inhibited by colchicine but does not require cytoplasmic microtubules. J. Cell Sci. 115:2002;3747-3756
-
(2002)
J. Cell Sci.
, vol.115
, pp. 3747-3756
-
-
Cowan, C.R.1
Cande, W.Z.2
-
39
-
-
23444456650
-
Synthesis and anticancer activity of new derivatives of podophyllotoxin
-
Cui Y.J., Tian X.A. Synthesis and anticancer activity of new derivatives of podophyllotoxin. Curr. Sci. 75:1998;1383-1386
-
(1998)
Curr. Sci.
, vol.75
, pp. 1383-1386
-
-
Cui, Y.J.1
Tian, X.A.2
-
40
-
-
0030989428
-
A one-pot, efficient synthesis of the potent cytotoxic podophyllotoxin derivative NPF
-
Daley L., Meresse P., Bertounesque E., Monneret C. A one-pot, efficient synthesis of the potent cytotoxic podophyllotoxin derivative NPF. Tetrahedron Lett. 38:1997;2673-2676
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 2673-2676
-
-
Daley, L.1
Meresse, P.2
Bertounesque, E.3
Monneret, C.4
-
41
-
-
0032487837
-
Synthesis and antitumor activity of new glycosides of epipodophyllotoxin, analogues of etoposide, and NK 611
-
Daley L., Guminski Y., Demerseman P., Kruczynski A., Etievant C., Imbert T., Hill B.T., Monneret C. Synthesis and antitumor activity of new glycosides of epipodophyllotoxin, analogues of etoposide, and NK 611. J. Med. Chem. 41:1998;4475-4485
-
(1998)
J. Med. Chem.
, vol.41
, pp. 4475-4485
-
-
Daley, L.1
Guminski, Y.2
Demerseman, P.3
Kruczynski, A.4
Etievant, C.5
Imbert, T.6
Hill, B.T.7
Monneret, C.8
-
42
-
-
0031810637
-
Podophyllotoxins: Current status and recent developments
-
Damayanthi Y., Lown J.W. Podophyllotoxins: current status and recent developments. Curr. Med. Chem. 5:1998;205-252
-
(1998)
Curr. Med. Chem.
, vol.5
, pp. 205-252
-
-
Damayanthi, Y.1
Lown, J.W.2
-
43
-
-
0034389321
-
Vinblastine-podophylotoxin, a good mitotic agent for preparing embryonic chromosomes
-
Datt M., Sharma A. Vinblastine-podophylotoxin, a good mitotic agent for preparing embryonic chromosomes. Ind. J. Anim. Sci. 70:2000;912-913
-
(2000)
Ind. J. Anim. Sci.
, vol.70
, pp. 912-913
-
-
Datt, M.1
Sharma, A.2
-
44
-
-
0031031957
-
Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center
-
Davin L.B., Wang H.B., Crowell A.L., Bedgar D.L., Martin D.M., Sarkanen S., Lewis N.G. Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center. Science. 275:1997;362-366
-
(1997)
Science
, vol.275
, pp. 362-366
-
-
Davin, L.B.1
Wang, H.B.2
Crowell, A.L.3
Bedgar, D.L.4
Martin, D.M.5
Sarkanen, S.6
Lewis, N.G.7
-
45
-
-
0036741230
-
Four lignans from Commiphora erlangeriana
-
Dekebo A., Lang M., Polborn K., Dagne E., Steglich W. Four lignans from Commiphora erlangeriana. J. Nat. Prod. 65:2002;1252-1257
-
(2002)
J. Nat. Prod.
, vol.65
, pp. 1252-1257
-
-
Dekebo, A.1
Lang, M.2
Polborn, K.3
Dagne, E.4
Steglich, W.5
-
46
-
-
10144260637
-
Dioxabicyclooctanyl naphthalenenitriles as nonredox 5-lipoxygenase inhibitors: Structure-activity relationship study directed toward the improvement of metabolic stability
-
Delorme D., Ducharme Y., Brideau C., Chan C.C., Chauret N., Desmarais S., Dube D., Falgueyret J.P., Fortin R., Guay J., Hamel P., Jones T.R., Lepine C., McAuliffe M., McFarlane C.S., Nicoll-Griffith D.A., Riendeau D., Yergey J.A., Girard Y. Dioxabicyclooctanyl naphthalenenitriles as nonredox 5-lipoxygenase inhibitors: structure-activity relationship study directed toward the improvement of metabolic stability. J. Med. Chem. 39:1996;3951-3970
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3951-3970
-
-
Delorme, D.1
Ducharme, Y.2
Brideau, C.3
Chan, C.C.4
Chauret, N.5
Desmarais, S.6
Dube, D.7
Falgueyret, J.P.8
Fortin, R.9
Guay, J.10
Hamel, P.11
Jones, T.R.12
Lepine, C.13
McAuliffe, M.14
McFarlane, C.S.15
Nicoll-Griffith, D.A.16
Riendeau, D.17
Yergey, J.A.18
Girard, Y.19
-
47
-
-
0042262526
-
Current status and future strategy for development of medicinal plants sector in Uttaranchal, India
-
Dhar U., Manjkhola S., Joshi M., Bhatt A., Bisht A.K., Joshi M. Current status and future strategy for development of medicinal plants sector in Uttaranchal, India. Curr. Sci. 83:2002;956-964
-
(2002)
Curr. Sci.
, vol.83
, pp. 956-964
-
-
Dhar, U.1
Manjkhola, S.2
Joshi, M.3
Bhatt, A.4
Bisht, A.K.5
Joshi, M.6
-
48
-
-
0026322408
-
Interference of epipodophyllotoxins and natural lignanolides with topoisomerase II: A proposed molecular mechanism
-
Eich E., Schulz J., Kaloga M., Merz H., Schoder H.C., Muller W.E.G. Interference of epipodophyllotoxins and natural lignanolides with topoisomerase II: a proposed molecular mechanism. Planta Med. 57:(Suppl. 2):1991;A7
-
(1991)
Planta Med.
, vol.57
, Issue.SUPPL. 2
, pp. 7
-
-
Eich, E.1
Schulz, J.2
Kaloga, M.3
Merz, H.4
Schoder, H.C.5
Muller, W.E.G.6
-
49
-
-
0030041593
-
(-)-Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase
-
Eich E., Pertz H., Kaloga M., Schulz J., Fesen M.R., Mazumder A., Pommier Y. (-)-Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase. J. Med. Chem. 39:1996;86-95
-
(1996)
J. Med. Chem.
, vol.39
, pp. 86-95
-
-
Eich, E.1
Pertz, H.2
Kaloga, M.3
Schulz, J.4
Fesen, M.R.5
Mazumder, A.6
Pommier, Y.7
-
50
-
-
0033831662
-
The use of plant cell cultures for the production of podophyllotoxin and related lignans
-
Empt U., Alfermann A.W., Pras N., Petersen M. The use of plant cell cultures for the production of podophyllotoxin and related lignans. J. Appl. Bot. 74:2000;145-150
-
(2000)
J. Appl. Bot.
, vol.74
, pp. 145-150
-
-
Empt, U.1
Alfermann, A.W.2
Pras, N.3
Petersen, M.4
-
51
-
-
0028115715
-
A phase III comparison of CHOP vs. m-BACOD vs. ProMACE-CytaBOM vs. MACOP-B in patients with intermediate- or high-grade non-Hodgkin's's lymphoma: Results of SWOG-8516 (Intergroup 0067), the national high-priority lymphoma study
-
Fisher R.I., Gaynor E.R., Dahlberg S., Oken M.M., Grogan T.M., Mize E.M., Glick J.M., Coltman C.A. Jr., Miller T.P. A phase III comparison of CHOP vs. m-BACOD vs. ProMACE-CytaBOM vs. MACOP-B in patients with intermediate- or high-grade non-Hodgkin's's lymphoma: results of SWOG-8516 (Intergroup 0067), the national high-priority lymphoma study. Ann. Oncol. 5:(Suppl 2):1994;91-95
-
(1994)
Ann. Oncol.
, vol.5
, Issue.SUPPL. 2
, pp. 91-95
-
-
Fisher, R.I.1
Gaynor, E.R.2
Dahlberg, S.3
Oken, M.M.4
Grogan, T.M.5
Mize, E.M.6
Glick, J.M.7
Coltman Jr., C.A.8
Miller, T.P.9
-
54
-
-
0035844716
-
Cycloisomerization of 1,6-enynes in organoaqueous medium: An efficient and eco-friendly access to furan derivatives. Synthesis of a key intermediate of podophyllotoxin
-
Galland J.C., Dias S., Savignac M., Genet J.P. Cycloisomerization of 1,6-enynes in organoaqueous medium: an efficient and eco-friendly access to furan derivatives. Synthesis of a key intermediate of podophyllotoxin. Tetrahedron. 57:2001;5137-5148
-
(2001)
Tetrahedron
, vol.57
, pp. 5137-5148
-
-
Galland, J.C.1
Dias, S.2
Savignac, M.3
Genet, J.P.4
-
55
-
-
0028090345
-
Inhibition of tumor necrosis factor-α (TNF-α) and interleukin-1 β (IL-1 β) secretion but not IL-6 from activated human peripheral blood monocytes by a new synthetic demethylpodophyllotoxin derivative
-
Gan X.H., Robin J.P., Mencia-Huerta J.M., Braquet P., Bonavida B. Inhibition of tumor necrosis factor-α (TNF-α) and interleukin-1 β (IL-1 β) secretion but not IL-6 from activated human peripheral blood monocytes by a new synthetic demethylpodophyllotoxin derivative. J. Clin. Immunol. 14:1994;280-288
-
(1994)
J. Clin. Immunol.
, vol.14
, pp. 280-288
-
-
Gan, X.H.1
Robin, J.P.2
Mencia-Huerta, J.M.3
Braquet, P.4
Bonavida, B.5
-
56
-
-
0032991637
-
Separation of Podophyllum lignans by micellar electrokinetic capillary chromatography (MECC)
-
Ganzera M., Moraes R.M., Khan I.A. Separation of Podophyllum lignans by micellar electrokinetic capillary chromatography (MECC). Chromatographia. 49:1999;552-556
-
(1999)
Chromatographia
, vol.49
, pp. 552-556
-
-
Ganzera, M.1
Moraes, R.M.2
Khan, I.A.3
-
58
-
-
0034735985
-
Effects of lignoids on a hematophagous bug. Rhodnius prolixus: Feeding, ecdysis and diuresis
-
Garcia E.S., Cabral M.M.O., Schaub G.A., Gottlieb O.R., Azambuja P. Effects of lignoids on a hematophagous bug. Rhodnius prolixus: feeding, ecdysis and diuresis. Phytochemistry. 55:2000;611-616
-
(2000)
Phytochemistry
, vol.55
, pp. 611-616
-
-
Garcia, E.S.1
Cabral, M.M.O.2
Schaub, G.A.3
Gottlieb, O.R.4
Azambuja, P.5
-
59
-
-
0037100142
-
A new approach toward the synthesis of heterolignans
-
Garzino F., Meou A., Brun P. A new approach toward the synthesis of heterolignans. Tetrahedron Lett. 43:2002;5049-5051
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 5049-5051
-
-
Garzino, F.1
Meou, A.2
Brun, P.3
-
60
-
-
0001365806
-
Cardiovascular activity of naturally occurring lignans
-
Ghisalberti E.L. Cardiovascular activity of naturally occurring lignans. Phytomedicine. 4:1997;151-166
-
(1997)
Phytomedicine
, vol.4
, pp. 151-166
-
-
Ghisalberti, E.L.1
-
61
-
-
0033744225
-
Production of podophyllotoxin from Podophyllum hexandrum: A potential natural product for clinically useful anticancer drugs
-
Giri A., Narasu M.L. Production of podophyllotoxin from Podophyllum hexandrum: a potential natural product for clinically useful anticancer drugs. Cytotechnology. 34:2000;17-26
-
(2000)
Cytotechnology
, vol.34
, pp. 17-26
-
-
Giri, A.1
Narasu, M.L.2
-
62
-
-
0034163670
-
Transgenic hairy rotos: Recent trends and applications
-
Giri A., Narasu M.L. Transgenic hairy rotos: recent trends and applications. Biotechnol. Adv. 18:2000;1-22
-
(2000)
Biotechnol. Adv.
, vol.18
, pp. 1-22
-
-
Giri, A.1
Narasu, M.L.2
-
64
-
-
0029098289
-
Synthesis and evaluation of pyrazolignans. A new class of cytotoxic agents
-
Gordaliza M., Miguel del Corral J.M., Castro M.A., López- Vázquez M.L., San Feliciano A., García-Grávalos M.D., Carpy A. Synthesis and evaluation of pyrazolignans. A new class of cytotoxic agents. Bioorg. Med. Chem. 3:1995;1203-1210
-
(1995)
Bioorg. Med. Chem.
, vol.3
, pp. 1203-1210
-
-
Gordaliza, M.1
Miguel Del Corral, J.M.2
Castro, M.A.3
López- Vázquez, M.L.4
San Feliciano, A.5
García-Grávalos, M.D.6
Carpy, A.7
-
65
-
-
0030785273
-
In vivo immunosuppressive activity of some cyclolignans
-
Gordaliza M., Castro M.A., Miguel del Corral J.M., López- Vázquez M.L., San Feliciano A., Faircloth G.T. In vivo immunosuppressive activity of some cyclolignans. Bioorg. Med. Chem. Lett. 7:1997;2781-2786
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 2781-2786
-
-
Gordaliza, M.1
Castro, M.A.2
Miguel Del Corral, J.M.3
López- Vázquez, M.L.4
San Feliciano, A.5
Faircloth, G.T.6
-
67
-
-
0033914099
-
Synthesis and antineoplastic activity of cyclolignan aldehydes
-
Gordaliza M., Castro M.A., Miguel del Corral J.M., López-Vazquez M.L., García P.A., García-Grávalos M.D., San Feliciano A. Synthesis and antineoplastic activity of cyclolignan aldehydes. Eur. J. Med. Chem. 35:2000;691-698
-
(2000)
Eur. J. Med. Chem.
, vol.35
, pp. 691-698
-
-
Gordaliza, M.1
Castro, M.A.2
Miguel Del Corral, J.M.3
López-Vazquez, M.L.4
García, P.A.5
García-Grávalos, M.D.6
San Feliciano, A.7
-
68
-
-
0035303594
-
Cytotoxic cyclolignans related to podophyllotoxin
-
Gordaliza M., Miguel del Corral J.M., Castro M.A., García- García P.A., San Feliciano A. Cytotoxic cyclolignans related to podophyllotoxin. Il Fármaco. 56:2001;297-304
-
(2001)
Il Fármaco
, vol.56
, pp. 297-304
-
-
Gordaliza, M.1
Miguel Del Corral, J.M.2
Castro, M.A.3
García- García, P.A.4
San Feliciano, A.5
-
69
-
-
0032878627
-
Drug delivery of anticancer agents: Water soluble 4-poly (ethylene glycol) derivatives of the lignan podophyllotoxin
-
Greenwald R.B., Conover C.D., Pendri A., Choe Y.H., Martinez A., Wu D.C., Guan S.Y., Yao Z.L., Shum K.L. Drug delivery of anticancer agents: water soluble 4-poly (ethylene glycol) derivatives of the lignan podophyllotoxin. J. Controlled Release. 61:1999;281-294
-
(1999)
J. Controlled Release
, vol.61
, pp. 281-294
-
-
Greenwald, R.B.1
Conover, C.D.2
Pendri, A.3
Choe, Y.H.4
Martinez, A.5
Wu, D.C.6
Guan, S.Y.7
Yao, Z.L.8
Shum, K.L.9
-
70
-
-
0036320742
-
Constituents of the twigs of Hernandia ovigera that inhibit the transformation of JB6 murine epidermal cells
-
Gu J.Q., Park E.J., Totura S., Riswan S., Fong H.H.S., Pezzuto J.M., Kinghorn A.D. Constituents of the twigs of Hernandia ovigera that inhibit the transformation of JB6 murine epidermal cells. J. Nat. Prod. 65:2002;1065-1068
-
(2002)
J. Nat. Prod.
, vol.65
, pp. 1065-1068
-
-
Gu, J.Q.1
Park, E.J.2
Totura, S.3
Riswan, S.4
Fong, H.H.S.5
Pezzuto, J.M.6
Kinghorn, A.D.7
-
71
-
-
0348013104
-
Synthesis of [60]fullerene-podophyllotoxin derivative
-
Guo L.W., Gao X., Zhang D.W., Wu S.H., Wu H.M. Synthesis of [60]fullerene-podophyllotoxin derivative. Chin. J. Chem. 20:2002;1430-1433
-
(2002)
Chin. J. Chem.
, vol.20
, pp. 1430-1433
-
-
Guo, L.W.1
Gao, X.2
Zhang, D.W.3
Wu, S.H.4
Wu, H.M.5
-
72
-
-
0029791770
-
Studies to show that with podophyllotoxin the early replicative stages of herpes simplex virus type 1 depend upon functional cytoplasmic microtubules
-
Hammonds T.R., Denyer S.P., Jackson D.E., Irving W.L. Studies to show that with podophyllotoxin the early replicative stages of herpes simplex virus type 1 depend upon functional cytoplasmic microtubules. J. Med. Microb. 45:1996;167-172
-
(1996)
J. Med. Microb.
, vol.45
, pp. 167-172
-
-
Hammonds, T.R.1
Denyer, S.P.2
Jackson, D.E.3
Irving, W.L.4
-
73
-
-
0030992580
-
Tetrahydronaphthalene lignan compounds as potent anti-HIV type 1 agents
-
Hara H., Fujihashi T., Sakata T., Kaji A., Kaji H. Tetrahydronaphthalene lignan compounds as potent anti-HIV type 1 agents. Aids Res. Hum. Retroviruses. 13:1997;695-705
-
(1997)
Aids Res. Hum. Retroviruses
, vol.13
, pp. 695-705
-
-
Hara, H.1
Fujihashi, T.2
Sakata, T.3
Kaji, A.4
Kaji, H.5
-
74
-
-
0031728637
-
Podophyllotoxin-induced acantholysis and cytolysis in a skin equivalent model
-
Hermanns L.T., Arrese J.E., Goffin V., Pierard G.E. Podophyllotoxin- induced acantholysis and cytolysis in a skin equivalent model. Eur. J. Morphol. 36:1998;183-187
-
(1998)
Eur. J. Morphol.
, vol.36
, pp. 183-187
-
-
Hermanns, L.T.1
Arrese, J.E.2
Goffin, V.3
Pierard, G.E.4
-
75
-
-
0033579609
-
Synthesis of (-)-4-aza-4-deoxypodophyllotoxin from (-)-podophyllotoxin
-
Hitotsuyanagi Y., Kobayashi M., Morita H., Itokawa H., Takeya K. Synthesis of (-)-4-aza-4-deoxypodophyllotoxin from (-)-podophyllotoxin. Tetrahedron Lett. 40:1999;9107-9110
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 9107-9110
-
-
Hitotsuyanagi, Y.1
Kobayashi, M.2
Morita, H.3
Itokawa, H.4
Takeya, K.5
-
76
-
-
0034696048
-
4-aza-2,3-dehydro-4-deoxypodophyllotoxins: Simple aza-podophyllotoxin analogues possessing potent cytotoxicity
-
Hitotsuyanagi Y., Fukuyo M., Tsuda K., Kobayashi M., Ozeki A., Itokawa H., Takeya K. 4-aza-2,3-dehydro-4-deoxypodophyllotoxins: simple aza-podophyllotoxin analogues possessing potent cytotoxicity. Bioorg. Med. Chem. Lett. 10:2000;315-317
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 315-317
-
-
Hitotsuyanagi, Y.1
Fukuyo, M.2
Tsuda, K.3
Kobayashi, M.4
Ozeki, A.5
Itokawa, H.6
Takeya, K.7
-
77
-
-
0032784679
-
A novel podophyllotoxin-derived compound GL331 is more potent than its congener VP-16 in killing refractory cancer cells
-
Huang T.S., Lee C.C., Chao Y., Shu C.H., Chen L.T., Chen L.L., Chen M.H., Yuan C., Whang-Peng J. A novel podophyllotoxin-derived compound GL331 is more potent than its congener VP-16 in killing refractory cancer cells. Pharmaceut. Res. 16:1999;997-1002
-
(1999)
Pharmaceut. Res.
, vol.16
, pp. 997-1002
-
-
Huang, T.S.1
Lee, C.C.2
Chao, Y.3
Shu, C.H.4
Chen, L.T.5
Chen, L.L.6
Chen, M.H.7
Yuan, C.8
Whang-Peng, J.9
-
78
-
-
0034018817
-
In vitro evaluation of GL331's cancer cell killing and apoptosis-inducing activity in combination with other chemotherapeutic agents
-
Huang T.S., Shu C.H., Lee C.C., Chen L.T., Whang-Peng J. In vitro evaluation of GL331's cancer cell killing and apoptosis-inducing activity in combination with other chemotherapeutic agents. Apoptosis. 5:2000;79-85
-
(2000)
Apoptosis
, vol.5
, pp. 79-85
-
-
Huang, T.S.1
Shu, C.H.2
Lee, C.C.3
Chen, L.T.4
Whang-Peng, J.5
-
79
-
-
0006760337
-
Practical route to introduce lexitropsins possessing a natural trisulfide linker; Synthesis of N-(lexitropsin-thiosulfenyl) phthalimides
-
Iida H., Lown J.W. Practical route to introduce lexitropsins possessing a natural trisulfide linker; synthesis of N-(lexitropsin-thiosulfenyl) phthalimides. Heterocyclic Commun. 4:1998;525-528
-
(1998)
Heterocyclic Commun.
, vol.4
, pp. 525-528
-
-
Iida, H.1
Lown, J.W.2
-
80
-
-
0034096523
-
Podophyllotoxin aza-analogue, a novel DNA topoisomerase II inhibitor
-
Iida A., Kano M., Kubota Y., Koga K., Tomioka K. Podophyllotoxin aza-analogue, a novel DNA topoisomerase II inhibitor. Chem. Pharm. Bull. 48:2000;486-489
-
(2000)
Chem. Pharm. Bull.
, vol.48
, pp. 486-489
-
-
Iida, A.1
Kano, M.2
Kubota, Y.3
Koga, K.4
Tomioka, K.5
-
81
-
-
0032033637
-
Discovery of podophyllotoxins
-
Imbert T.F. Discovery of podophyllotoxins. Biochimie. 80:1998;207-222
-
(1998)
Biochimie
, vol.80
, pp. 207-222
-
-
Imbert, T.F.1
-
82
-
-
0023022149
-
The biological activities of podophyllotoxin compounds
-
Inamori Y., Kubo M., Tsujibo H., Ogawa M., Baba K., Kozawa M., Fujita E. The biological activities of podophyllotoxin compounds. Chem. Pharm. Bull. 34:1986;3928-3932
-
(1986)
Chem. Pharm. Bull.
, vol.34
, pp. 3928-3932
-
-
Inamori, Y.1
Kubo, M.2
Tsujibo, H.3
Ogawa, M.4
Baba, K.5
Kozawa, M.6
Fujita, E.7
-
83
-
-
0028846502
-
Arylnaphthalene lignans as novel series of hypolipidemic agents raising high-density lipoprotein level
-
Iwasaki T., Kondo K., Nishitani T., Kuroda T., Hirakoso K., Ohtani A., Takashima K. Arylnaphthalene lignans as novel series of hypolipidemic agents raising high-density lipoprotein level. Chem. Pharm. Bull. 43:1995;1701-1705
-
(1995)
Chem. Pharm. Bull.
, vol.43
, pp. 1701-1705
-
-
Iwasaki, T.1
Kondo, K.2
Nishitani, T.3
Kuroda, T.4
Hirakoso, K.5
Ohtani, A.6
Takashima, K.7
-
84
-
-
0029945418
-
Novel selective PDE IV inhibitors as antiasthmatic agents. Synthesis and biological activities of a series of 1-aryl-2,3-bis(hydroxymethyl) naphthalene lignans
-
Iwasaki T., Kondo K., Kuroda T., Moritani Y., Yamagata M., Sugiura H., Kikkawa H., Kaminuma O., Ikezawa K. Novel selective PDE IV inhibitors as antiasthmatic agents. Synthesis and biological activities of a series of 1-aryl-2,3-bis(hydroxymethyl) naphthalene lignans. J. Med. Chem. 39:1996;2696-2704
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2696-2704
-
-
Iwasaki, T.1
Kondo, K.2
Kuroda, T.3
Moritani, Y.4
Yamagata, M.5
Sugiura, H.6
Kikkawa, H.7
Kaminuma, O.8
Ikezawa, K.9
-
85
-
-
0342930999
-
Aryltetralin lignans from Podophyllum hexandrum and Podophyllum peltatum
-
Jackson D.E., Dewick P.M. Aryltetralin lignans from Podophyllum hexandrum and Podophyllum peltatum. Phytochemistry. 23:1984;1147-1152
-
(1984)
Phytochemistry
, vol.23
, pp. 1147-1152
-
-
Jackson, D.E.1
Dewick, P.M.2
-
86
-
-
0033012947
-
Action of free radical in podophyllic acid piperindyl hydrazone nitroxide radical on its antitumor activity and toxicity
-
Jia Z.P., Wang R., Xie J.W., Xu L.T. Action of free radical in podophyllic acid piperindyl hydrazone nitroxide radical on its antitumor activity and toxicity. Acta Pharm. Sin. 20:1999;571-576
-
(1999)
Acta Pharm. Sin.
, vol.20
, pp. 571-576
-
-
Jia, Z.P.1
Wang, R.2
Xie, J.W.3
Xu, L.T.4
-
87
-
-
0032815538
-
Synthesis and spectral characteristics of some unusual fatty esters of podophyllotoxin
-
Jie M.S.F.L.K., Mustafa J., Pasha M.K. Synthesis and spectral characteristics of some unusual fatty esters of podophyllotoxin. Chem. Phys. Lipids. 100:1999;165-170
-
(1999)
Chem. Phys. Lipids
, vol.100
, pp. 165-170
-
-
Jie, M.S.F.L.K.1
Mustafa, J.2
Pasha, M.K.3
-
88
-
-
0033812998
-
Facile and efficient one-pot synthesis of 4β-arylamino- podophyllotoxins: Synthesis of DNA topoisomerase II inhibitors (NPF and W-68)
-
Kamal A., Laxman N., Ramesh G. Facile and efficient one-pot synthesis of 4β-arylamino-podophyllotoxins: synthesis of DNA topoisomerase II inhibitors (NPF and W-68). Bioorg. Med. Chem. Lett. 10:2000;2059-2062
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2059-2062
-
-
Kamal, A.1
Laxman, N.2
Ramesh, G.3
-
89
-
-
0033613889
-
Stereospecific synthesis of oxazolo[3,4-b]tetrahydroisoquinolin-3-ones, analogs of podophyllotoxin, via benzotriazole methodology
-
Katritzky A.R., Cobo-Domingo J., Yang B.Z., Steel P.J. Stereospecific synthesis of oxazolo[3,4-b]tetrahydroisoquinolin-3-ones, analogs of podophyllotoxin, via benzotriazole methodology. Tetrahedron: Asymmetry. 10:1999;255-263
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 255-263
-
-
Katritzky, A.R.1
Cobo-Domingo, J.2
Yang, B.Z.3
Steel, P.J.4
-
90
-
-
0036888356
-
Prodrugs of 4′-demethyl-4-deoxypodophyllotoxin: Synthesis and evaluation of the antitumor activity
-
Kim Y., You Y.J., Nam N.H., Ahn B.Z. Prodrugs of 4′-demethyl-4- deoxypodophyllotoxin: synthesis and evaluation of the antitumor activity. Bioorg. Med. Chem. 2:2002;3435-3438
-
(2002)
Bioorg. Med. Chem.
, vol.2
, pp. 3435-3438
-
-
Kim, Y.1
You, Y.J.2
Nam, N.H.3
Ahn, B.Z.4
-
91
-
-
0031005741
-
Synthesis and hypolipidemic activity of diesters of arylnaphthalene lignan and their heteroaromatic analogs
-
Kuroda T., Kondo K., Iwasaki T., Ohtani A., Takashima K. Synthesis and hypolipidemic activity of diesters of arylnaphthalene lignan and their heteroaromatic analogs. Chem. Pharm. Bull. 45:1997;678-684
-
(1997)
Chem. Pharm. Bull.
, vol.45
, pp. 678-684
-
-
Kuroda, T.1
Kondo, K.2
Iwasaki, T.3
Ohtani, A.4
Takashima, K.5
-
92
-
-
4043171726
-
Biotechnology and synthetic chemistry - Routes to clinically important compounds
-
Kutney J.P. Biotechnology and synthetic chemistry - routes to clinically important compounds. Pure Appl. Chem. 71:1999;1025-1032
-
(1999)
Pure Appl. Chem.
, vol.71
, pp. 1025-1032
-
-
Kutney, J.P.1
-
93
-
-
0023228479
-
Comparison of podophyllotoxin and podophyllin in treatment of genital warts
-
Lassus A. Comparison of podophyllotoxin and podophyllin in treatment of genital warts. Lancet. 2:1987;512-513
-
(1987)
Lancet
, vol.2
, pp. 512-513
-
-
Lassus, A.1
-
94
-
-
4043120848
-
-
Medicinal used for podophyllotoxin. US patent, 4,788,216.
-
K. Leander, B. Rosen, 1988. Medicinal used for podophyllotoxin. US patent, 4,788,216.
-
(1988)
-
-
Leander, K.1
Rosen, B.2
-
95
-
-
0344994511
-
Novel antitumor agents from higher plants
-
Lee K.H. Novel antitumor agents from higher plants. Med. Res. Rev. 19:1999;569-596
-
(1999)
Med. Res. Rev.
, vol.19
, pp. 569-596
-
-
Lee, K.H.1
-
96
-
-
0034858972
-
A novel topoisomerase II poison GL331 preferentially induces DNA cleavage at (C/G) T sites and can cause telomere DNA damage
-
Lee C.C., Huang T.S. A novel topoisomerase II poison GL331 preferentially induces DNA cleavage at (C/G) T sites and can cause telomere DNA damage. Acta Pharm. Res. 18:2001;846-851
-
(2001)
Acta Pharm. Res.
, vol.18
, pp. 846-851
-
-
Lee, C.C.1
Huang, T.S.2
-
97
-
-
0030694262
-
Anti-AIDS agents. 29. Anti-HIV activity of modified podophyllotoxin derivatives
-
Lee C.T.L., Lin V.C.K., Zhang S.X., Zhu X.K., Vliet D.V., Hu H., Beers S.A., Wang Z.Q., Cosentino L.M., Morris-Natschke S.L., Lee K.H. Anti-AIDS agents. 29. Anti-HIV activity of modified podophyllotoxin derivatives. Bioorg. Med. Chem. Lett. 7:1997;2897-2902
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 2897-2902
-
-
Lee, C.T.L.1
Lin, V.C.K.2
Zhang, S.X.3
Zhu, X.K.4
Vliet, D.V.5
Hu, H.6
Beers, S.A.7
Wang, Z.Q.8
Cosentino, L.M.9
Morris-Natschke, S.L.10
Lee, K.H.11
-
98
-
-
0032762321
-
Studies on pyrrolidinone. Synthesis of aza analogs of podophyllotoxin and related compounds
-
Legrand A., Rigo B., Gautret P., Henichart J.P., Couturier D. Studies on pyrrolidinone. Synthesis of aza analogs of podophyllotoxin and related compounds. J. Heterocyclic Chem. 36:1999;1263-1270
-
(1999)
J. Heterocyclic Chem.
, vol.36
, pp. 1263-1270
-
-
Legrand, A.1
Rigo, B.2
Gautret, P.3
Henichart, J.P.4
Couturier, D.5
-
99
-
-
0034032210
-
A clinical study of CPH 82 vs. methotrexate in early rheumatoid arthritis
-
Lerndal T., Svensson B. A clinical study of CPH 82 vs. methotrexate in early rheumatoid arthritis. Rheumatology (Oxford). 39:2000;316-320
-
(2000)
Rheumatology (Oxford)
, vol.39
, pp. 316-320
-
-
Lerndal, T.1
Svensson, B.2
-
100
-
-
0036023604
-
Antioxidative activity of spin labeled derivatives of podophyllic acid hydrazide
-
Li W.G., Zhang X.Y., Wu Y.J., Tian X.A. Antioxidative activity of spin labeled derivatives of podophyllic acid hydrazide. Acta Pharm. Sin. 23:2002;727-732
-
(2002)
Acta Pharm. Sin.
, vol.23
, pp. 727-732
-
-
Li, W.G.1
Zhang, X.Y.2
Wu, Y.J.3
Tian, X.A.4
-
101
-
-
0033109616
-
Cytotoxic constituents from the roots of Anthriscus sylvestris
-
Lim Y.H., Leem M.J., Shin D.H., Chang H.B., Hong S.W., Moon E.Y., Lee D.K., Yoon S.J., Woo W.S. Cytotoxic constituents from the roots of Anthriscus sylvestris. Arch. Pharmacol. Res. 22:1999;208-212
-
(1999)
Arch. Pharmacol. Res.
, vol.22
, pp. 208-212
-
-
Lim, Y.H.1
Leem, M.J.2
Shin, D.H.3
Chang, H.B.4
Hong, S.W.5
Moon, E.Y.6
Lee, D.K.7
Yoon, S.J.8
Woo, W.S.9
-
102
-
-
0034802324
-
GL331 induces down-regulation of cyclin D1 expression via enhanced proteolysis and repressed transcription
-
Lin S.K., Huang H.C., Chen L.L., Lee C.C., Huang T.S. GL331 induces down-regulation of cyclin D1 expression via enhanced proteolysis and repressed transcription. Mol. Pharmacol. 60:2001;768-775
-
(2001)
Mol. Pharmacol.
, vol.60
, pp. 768-775
-
-
Lin, S.K.1
Huang, H.C.2
Chen, L.L.3
Lee, C.C.4
Huang, T.S.5
-
103
-
-
0001501234
-
Lignans and tannins as inhibitors of viral reverse transcriptase and human DNA polymerase-α: QSAR analysis and molecular modeling
-
Liu K.C.S.C., Lee S.S., Lin M.T., Chang C.W., Liu C.L., Lin J.Y., Hsu F.L., Ren S., Lien E.J. Lignans and tannins as inhibitors of viral reverse transcriptase and human DNA polymerase-α: QSAR analysis and molecular modeling. Med. Chem. Res. 7:1997;168-179
-
(1997)
Med. Chem. Res.
, vol.7
, pp. 168-179
-
-
Liu, K.C.S.C.1
Lee, S.S.2
Lin, M.T.3
Chang, C.W.4
Liu, C.L.5
Lin, J.Y.6
Hsu, F.L.7
Ren, S.8
Lien, E.J.9
-
104
-
-
0035979709
-
Separation and determination of podophyllum lignans by micellar electrokinetic chromatography
-
Liu S.H., Tian X., Chen X.G., Hu Z.D. Separation and determination of podophyllum lignans by micellar electrokinetic chromatography. J. Chromatography. 928:2001;109-115
-
(2001)
J. Chromatography
, vol.928
, pp. 109-115
-
-
Liu, S.H.1
Tian, X.2
Chen, X.G.3
Hu, Z.D.4
-
105
-
-
0036907176
-
Micellar electrokinetic capillary chromatographic separation of diastereoisomers of podophyllum lignans at the C4 position
-
Liu S.H., Tian X., Chen X.G., Hu Z.D. Micellar electrokinetic capillary chromatographic separation of diastereoisomers of podophyllum lignans at the C4 position. Chromatographia. 56:2002;687-691
-
(2002)
Chromatographia
, vol.56
, pp. 687-691
-
-
Liu, S.H.1
Tian, X.2
Chen, X.G.3
Hu, Z.D.4
-
106
-
-
0037076694
-
Separation of diastereoisomers of podophyllum lignans by micellar electrokinetic chromatography
-
Liu S.H., Tian X., Chen X.G., Hu Z.D. Separation of diastereoisomers of podophyllum lignans by micellar electrokinetic chromatography. J. Chromatography. 959:2002;263-268
-
(2002)
J. Chromatography
, vol.959
, pp. 263-268
-
-
Liu, S.H.1
Tian, X.2
Chen, X.G.3
Hu, Z.D.4
-
107
-
-
4043157497
-
Aza-podophyllotoxin as potent cytotoxic agents
-
Lloyd A.W. Aza-podophyllotoxin as potent cytotoxic agents. Drug Discov. Today. 5:2000;260
-
(2000)
Drug Discov. Today
, vol.5
, pp. 260
-
-
Lloyd, A.W.1
-
108
-
-
0343526798
-
A role for dipole moment in the activity of cyclolignans
-
López-Pérez J.L., del Olmo E., de Pascual Teresa B., Merino M., Barajas M., San Feliciano A. A role for dipole moment in the activity of cyclolignans. J. Mol. Struct. (Theochem). 504:2000;51-57
-
(2000)
J. Mol. Struct. (Theochem)
, vol.504
, pp. 51-57
-
-
López-Pérez, J.L.1
Del Olmo, E.2
De Pascual Teresa, B.3
Merino, M.4
Barajas, M.5
San Feliciano, A.6
-
109
-
-
0342948492
-
-
M. Potmensil, & K.W. Kohn. New York: Oxford University Press
-
Mac Donald T.L., Lehnert E.K., Loper J.T., Chow K.C., Ross W.E. Potmensil M., Kohn K.W. DNA Topoisomerase in Cancer. 1992;Oxford University Press, New York
-
(1992)
DNA Topoisomerase in Cancer
-
-
Mac Donald, T.L.1
Lehnert, E.K.2
Loper, J.T.3
Chow, K.C.4
Ross, W.E.5
-
111
-
-
0034995845
-
Synthesis of imidazo[4,5-d]oxazolo[3,4-a]pyridines. New heterocyclic analogues of lignans
-
Madrigal B., Puebla P., Caballero E., Pelaez R., Gravalos D.G., Medarde M. Synthesis of imidazo[4,5-d]oxazolo[3,4-a]pyridines. New heterocyclic analogues of lignans. Arch. Pharm. 334:2001;177-179
-
(2001)
Arch. Pharm.
, vol.334
, pp. 177-179
-
-
Madrigal, B.1
Puebla, P.2
Caballero, E.3
Pelaez, R.4
Gravalos, D.G.5
Medarde, M.6
-
112
-
-
0037423353
-
Naphthalene analogues of lignans
-
Madrigal B., Puebla P., Pelaez R., Caballero E., Medarde M. Naphthalene analogues of lignans. J. Org. Chem. 68:2003;854-864
-
(2003)
J. Org. Chem.
, vol.68
, pp. 854-864
-
-
Madrigal, B.1
Puebla, P.2
Pelaez, R.3
Caballero, E.4
Medarde, M.5
-
113
-
-
4043171727
-
Mayapple: A review of the literature from a horticultural perspective. Annual Report of the North Mississippi Research and Extension Center
-
Maqbool M., Cushman K.E., Moraes R.M. Mayapple: a review of the literature from a horticultural perspective. Annual Report of the North Mississippi Research and Extension Center. Miss. Agric. For. Expt Sta. Info. Bull. 375:2001;313-319
-
(2001)
Miss. Agric. For. Expt Sta. Info. Bull.
, vol.375
, pp. 313-319
-
-
Maqbool, M.1
Cushman, K.E.2
Moraes, R.M.3
-
114
-
-
0035204088
-
The successful treatment of Molluscum contagiosum with podophyllotoxin (0.5%) self-application
-
Markos A.R. The successful treatment of Molluscum contagiosum with podophyllotoxin (0.5%) self-application. Int. J. STD AIDS. 12:2001;833
-
(2001)
Int. J. STD AIDS
, vol.12
, pp. 833
-
-
Markos, A.R.1
-
116
-
-
0036292462
-
Flow cytometric estimation on cytotoxic activity of leaf extracts from seashore plants in subtropical Japan: Isolation, quantification and cytotoxic action of (-)-deoxypodophyllotoxin
-
Masuda T., Oyama Y., Yonemori S., Takeda Y., Yamazaki Y., Mizuguchi S., Nakata M., Tanaka T., Chikahisa L., Inaba Y., Okada Y. Flow cytometric estimation on cytotoxic activity of leaf extracts from seashore plants in subtropical Japan: Isolation, quantification and cytotoxic action of (-)-deoxypodophyllotoxin. Phytother. Res. 16:2002;353-358
-
(2002)
Phytother. Res.
, vol.16
, pp. 353-358
-
-
Masuda, T.1
Oyama, Y.2
Yonemori, S.3
Takeda, Y.4
Yamazaki, Y.5
Mizuguchi, S.6
Nakata, M.7
Tanaka, T.8
Chikahisa, L.9
Inaba, Y.10
Okada, Y.11
-
117
-
-
0034907651
-
An alternative route to the synthesis of lignans intermediates
-
Masunari A., Ishida E., Trazzi G., Almeida W.P., Coelho F. An alternative route to the synthesis of lignans intermediates. Synth. Commun. 31:2001;2127-2136
-
(2001)
Synth. Commun.
, vol.31
, pp. 2127-2136
-
-
Masunari, A.1
Ishida, E.2
Trazzi, G.3
Almeida, W.P.4
Coelho, F.5
-
118
-
-
0033615756
-
Synthetic approaches to condensed aromatic analogues from etoposide, synthesis of A-ring pyridazine picroetoposide
-
Meresse P., Bertounesque E., Imbert T., Monneret C. Synthetic approaches to condensed aromatic analogues from etoposide, synthesis of A-ring pyridazine picroetoposide. Tetrahedron. 55:1999;12805-12818
-
(1999)
Tetrahedron
, vol.55
, pp. 12805-12818
-
-
Meresse, P.1
Bertounesque, E.2
Imbert, T.3
Monneret, C.4
-
120
-
-
0034929575
-
Influence of Podophyllum hexandrum on endogenous antioxidant defence system in mice: Possible role in radioprotection
-
Mittal A., Pathania V., Agrawala P.K., Prasad J., Singh S., Goel H.C. Influence of Podophyllum hexandrum on endogenous antioxidant defence system in mice: possible role in radioprotection. J. Ethnopharmacol. 76:2001;253-262
-
(2001)
J. Ethnopharmacol.
, vol.76
, pp. 253-262
-
-
Mittal, A.1
Pathania, V.2
Agrawala, P.K.3
Prasad, J.4
Singh, S.5
Goel, H.C.6
-
121
-
-
0346315935
-
Extractives of Juniperus chinensis L. - I: Isolation of podophyllotoxin and yatein from the leaves of J. chinensis
-
Miyata L., Itoh K., Tachibana S. Extractives of Juniperus chinensis L. - I: isolation of podophyllotoxin and yatein from the leaves of J. chinensis. J. Wood Sci. 44:1998;397-400
-
(1998)
J. Wood Sci.
, vol.44
, pp. 397-400
-
-
Miyata, L.1
Itoh, K.2
Tachibana, S.3
-
122
-
-
0033376949
-
Biologically active components against Drosophila melanogaster from Podophyllum hexandrum
-
Miyazawa M., Fukuyama M., Yoshio K., Kato T., Ishikawa Y. Biologically active components against Drosophila melanogaster from Podophyllum hexandrum. J. Agric. Food Chem. 47:1999;5108-5110
-
(1999)
J. Agric. Food Chem.
, vol.47
, pp. 5108-5110
-
-
Miyazawa, M.1
Fukuyama, M.2
Yoshio, K.3
Kato, T.4
Ishikawa, Y.5
-
123
-
-
0141465299
-
Deoxypodophyllotoxin 6-hydroxylase, a cytochrome P450 monooxygenase from cell cultures of Linum flavum involved in the biosynthesis of cytotoxic lignans
-
Molog G.A., Empt U., Kuhlmann S., van Uden W., Pras N., Alfermann A.W., Petersen M. Deoxypodophyllotoxin 6-hydroxylase, a cytochrome P450 monooxygenase from cell cultures of Linum flavum involved in the biosynthesis of cytotoxic lignans. Planta. 214:2001;288-294
-
(2001)
Planta
, vol.214
, pp. 288-294
-
-
Molog, G.A.1
Empt, U.2
Kuhlmann, S.3
Van Uden, W.4
Pras, N.5
Alfermann, A.W.6
Petersen, M.7
-
124
-
-
0034473699
-
The american mayapple revisited - Podophyllum peltatum - Still a potential cash crop?
-
Moraes R.M., Burandt C. Jr., Ganzera M., Li X., Khan I., Canel C. The american mayapple revisited - Podophyllum peltatum - still a potential cash crop? Econ. Bot. 54:2001;471-476
-
(2001)
Econ. Bot.
, vol.54
, pp. 471-476
-
-
Moraes, R.M.1
Burandt Jr., C.2
Ganzera, M.3
Li, X.4
Khan, I.5
Canel, C.6
-
125
-
-
0036248058
-
Evaluation of Podophyllum peltatum accessions for podophyllotoxin production
-
Moraes R.M., Bedir E., Barrett H., Burandt C., Canel C., Khan I.A. Evaluation of Podophyllum peltatum accessions for podophyllotoxin production. Planta Med. 68:2002;341-344
-
(2002)
Planta Med.
, vol.68
, pp. 341-344
-
-
Moraes, R.M.1
Bedir, E.2
Barrett, H.3
Burandt, C.4
Canel, C.5
Khan, I.A.6
-
126
-
-
0031985428
-
In vitro propagation of P. peltatum
-
Moraes-Cedeira R.M., Burandt C.L. Jr., Bastos J.K., Nanayakkara N.P.D., McChesney J.D. In vitro propagation of P. peltatum. Planta Med. 64:1998;42-46
-
(1998)
Planta Med.
, vol.64
, pp. 42-46
-
-
Moraes-Cedeira, R.M.1
Burandt Jr., C.L.2
Bastos, J.K.3
Nanayakkara, N.P.D.4
McChesney, J.D.5
-
127
-
-
0034583327
-
Nomenclature of lignans and neolignans
-
Moss G.P. Nomenclature of lignans and neolignans. Pure Appl. Chem. 72:2000;1493-1523
-
(2000)
Pure Appl. Chem.
, vol.72
, pp. 1493-1523
-
-
Moss, G.P.1
-
128
-
-
0033990519
-
Propagation and conservation of Podophyllum hexandrum Royle: An important medicinal herb
-
Nadeem M., Palni L.M.S., Purohit A.N., Pandey H., Nandi S.K. Propagation and conservation of Podophyllum hexandrum Royle: an important medicinal herb. Biol. Conserv. 92:2000;121-129
-
(2000)
Biol. Conserv.
, vol.92
, pp. 121-129
-
-
Nadeem, M.1
Palni, L.M.S.2
Purohit, A.N.3
Pandey, H.4
Nandi, S.K.5
-
129
-
-
0034070151
-
Tetralone esters as intermediates for the synthesis of podophyllotoxin derivatives via cyclopropanation of chalcones
-
Nanjundaswamy N., Shashikanth S., Anjanamurthy C., Rai K.M.L. Tetralone esters as intermediates for the synthesis of podophyllotoxin derivatives via cyclopropanation of chalcones. Synth. Commun. 30:2000;1179-1191
-
(2000)
Synth. Commun.
, vol.30
, pp. 1179-1191
-
-
Nanjundaswamy, N.1
Shashikanth, S.2
Anjanamurthy, C.3
Rai, K.M.L.4
-
130
-
-
0036275184
-
Synthesis of podophyllotoxin analogues. XII. Synthesis of β-apopicropodophyllin analogues
-
Nanjundaswamy N., Shashikanth S., Anjanamurthy C., Rai K.M.L. Synthesis of podophyllotoxin analogues. XII. Synthesis of β-apopicropodophyllin analogues. Synth. Commun. 32:2002;1475-1482
-
(2002)
Synth. Commun.
, vol.32
, pp. 1475-1482
-
-
Nanjundaswamy, N.1
Shashikanth, S.2
Anjanamurthy, C.3
Rai, K.M.L.4
-
131
-
-
0036355434
-
Aryltetralin lignans inhibit plant growth by affecting the formation of mitotic microtubular organizing centers
-
Oliva A., Moraes R.M., Watson S.B., Duke S.O., Dayan F.E. Aryltetralin lignans inhibit plant growth by affecting the formation of mitotic microtubular organizing centers. Pestic. Biochem. Physiol. 72:2002;45-54
-
(2002)
Pestic. Biochem. Physiol.
, vol.72
, pp. 45-54
-
-
Oliva, A.1
Moraes, R.M.2
Watson, S.B.3
Duke, S.O.4
Dayan, F.E.5
-
132
-
-
0001367283
-
Establishment of hairy root cultures of Linum flavum producing the lignan 5-methoxy podophyllotoxin
-
Oostdam A., Mol J.N.M., Vanderplas L.H.W. Establishment of hairy root cultures of Linum flavum producing the lignan 5-methoxy podophyllotoxin. Plant Cell Rep. 12:1993;474-477
-
(1993)
Plant Cell Rep.
, vol.12
, pp. 474-477
-
-
Oostdam, A.1
Mol, J.N.M.2
Vanderplas, L.H.W.3
-
133
-
-
0035951067
-
Conformational properties of α-tubulin tail peptide: Implications for a tail-body interaction
-
Pal D., Mahapatra P., Manna T., Chakrabarti P., Bhattacharyya B., Banerjee A., Basu G., Roy S. Conformational properties of α-tubulin tail peptide: implications for a tail-body interaction. Biochemistry. 40:2001;15512-15519
-
(2001)
Biochemistry
, vol.40
, pp. 15512-15519
-
-
Pal, D.1
Mahapatra, P.2
Manna, T.3
Chakrabarti, P.4
Bhattacharyya, B.5
Banerjee, A.6
Basu, G.7
Roy, S.8
-
134
-
-
0035689587
-
GA(3) induced flowering in Podophyllum hexandrum Royle: A rare alpine medicinal herb
-
Pandey H., Nandi S.K., Chandra B., Nadeem M., Palni L.M.S. GA(3) induced flowering in Podophyllum hexandrum Royle: a rare alpine medicinal herb. Acta Physiol. Plant. 23:2001;467-474
-
(2001)
Acta Physiol. Plant.
, vol.23
, pp. 467-474
-
-
Pandey, H.1
Nandi, S.K.2
Chandra, B.3
Nadeem, M.4
Palni, L.M.S.5
-
135
-
-
0035095071
-
The production of cytotoxic lignans by plant cell cultures
-
Petersen M., Alfermann A.W. The production of cytotoxic lignans by plant cell cultures. Appl. Microbiol. Biotechnol. 55:2001;135-142
-
(2001)
Appl. Microbiol. Biotechnol.
, vol.55
, pp. 135-142
-
-
Petersen, M.1
Alfermann, A.W.2
-
136
-
-
0037184777
-
An epiisopicropodophyllin aza analogue via palladium-catalyzed pseudo-domino cyclization
-
Poli G., Giambastiani G. An epiisopicropodophyllin aza analogue via palladium-catalyzed pseudo-domino cyclization. J. Org. Chem. 67:2002;9456-9459
-
(2002)
J. Org. Chem.
, vol.67
, pp. 9456-9459
-
-
Poli, G.1
Giambastiani, G.2
-
137
-
-
0035073578
-
Podophyllotoxin lignans enhance IL-1E but suppress TNF-a mRNA expression in LPS-treated monocytes
-
Pugh N.I., Khan I., Moraes R.M., Pasco D. Podophyllotoxin lignans enhance IL-1E but suppress TNF-a mRNA expression in LPS-treated monocytes. Immunopharmacol. Immunotoxicol. 23:2001;83-95
-
(2001)
Immunopharmacol. Immunotoxicol.
, vol.23
, pp. 83-95
-
-
Pugh, N.I.1
Khan, I.2
Moraes, R.M.3
Pasco, D.4
-
138
-
-
0036146609
-
Production of lignans by Haplophyllum patavinum in vivo and in vitro
-
Puricelli L., Innocenti G., Piacente S., Caniato R., Filippini R., Capelletti E.M. Production of lignans by Haplophyllum patavinum in vivo and in vitro. Heterocycles. 56:2002;607-612
-
(2002)
Heterocycles
, vol.56
, pp. 607-612
-
-
Puricelli, L.1
Innocenti, G.2
Piacente, S.3
Caniato, R.4
Filippini, R.5
Capelletti, E.M.6
-
139
-
-
0007323238
-
Variation in podophylloresin and podophyllotoxin contents in different populations of Podophyllum hexandrum
-
Purohit M.C., Bahuguna R., Maithani U.C., Purohit A.N., Rawat M.S.M. Variation in podophylloresin and podophyllotoxin contents in different populations of Podophyllum hexandrum. Curr. Sci. 77:1999;1078-1080
-
(1999)
Curr. Sci.
, vol.77
, pp. 1078-1080
-
-
Purohit, M.C.1
Bahuguna, R.2
Maithani, U.C.3
Purohit, A.N.4
Rawat, M.S.M.5
-
141
-
-
0035971846
-
Heterolignanolides, Furo- and thieno-analogues of podophyllotoxin and thuriferic acid
-
Ramos A.C., Pelaez R., Lopez J.L., Caballero E., Medarde M., San Feliciano A. Heterolignanolides, Furo- and thieno-analogues of podophyllotoxin and thuriferic acid. Tetrahedron. 57:2001;3963-3977
-
(2001)
Tetrahedron
, vol.57
, pp. 3963-3977
-
-
Ramos, A.C.1
Pelaez, R.2
Lopez, J.L.3
Caballero, E.4
Medarde, M.5
San Feliciano, A.6
-
143
-
-
6544271428
-
Phase I clinical and pharmacokinetic trial of the podophyllotoxin derivative NK611 administered as intravenous short infusion
-
Rassmann I., Thodtmann R., Mross M., Huttmann A., Berdel W.E., Manegold C., Fiebig H.H., Kaeser-Frohlich A., Burk K., Hanauske A.R. Phase I clinical and pharmacokinetic trial of the podophyllotoxin derivative NK611 administered as intravenous short infusion. Invest. New Drugs. 16:1998;319-324
-
(1998)
Invest. New Drugs
, vol.16
, pp. 319-324
-
-
Rassmann, I.1
Thodtmann, R.2
Mross, M.3
Huttmann, A.4
Berdel, W.E.5
Manegold, C.6
Fiebig, H.H.7
Kaeser-Frohlich, A.8
Burk, K.9
Hanauske, A.R.10
-
145
-
-
0036836668
-
Hemi-synthesis and biological activity of new analogues of podophyllotoxin
-
Roulland E., Magiatis P., Arimondo P., Bertounesque E., Monneret C. Hemi-synthesis and biological activity of new analogues of podophyllotoxin. Bioorg. Med. Chem. 10:2002;3463-3471
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 3463-3471
-
-
Roulland, E.1
Magiatis, P.2
Arimondo, P.3
Bertounesque, E.4
Monneret, C.5
-
147
-
-
0036277972
-
Protection against radiation induced damage to spermatogenesis by Podophyllum hexandrum
-
Samanta N., Goel H.C. Protection against radiation induced damage to spermatogenesis by Podophyllum hexandrum. J. Ethnopharmacol. 81:2002;217-224
-
(2002)
J. Ethnopharmacol.
, vol.81
, pp. 217-224
-
-
Samanta, N.1
Goel, H.C.2
-
148
-
-
0030477322
-
Etoposide phosphate: What, why, where, and how?
-
Schacter L. Etoposide phosphate: what, why, where, and how? Semin. Oncol. 6:(Suppl 13):1996;1-7
-
(1996)
Semin. Oncol.
, vol.6
, Issue.SUPPL. 13
, pp. 1-7
-
-
Schacter, L.1
-
149
-
-
0342470417
-
Crystallization of a macromolecular ring assembly of tubulin liganded with the anti-mitotic drug podophyllotoxin
-
Schonbrunn E., Phlippen W., Trinczek B., Sack S., Eschenburg S., Mandelkow E.M., Mandelkow E. Crystallization of a macromolecular ring assembly of tubulin liganded with the anti-mitotic drug podophyllotoxin. J. Struct. Biol. 128:1999;211-215
-
(1999)
J. Struct. Biol.
, vol.128
, pp. 211-215
-
-
Schonbrunn, E.1
Phlippen, W.2
Trinczek, B.3
Sack, S.4
Eschenburg, S.5
Mandelkow, E.M.6
Mandelkow, E.7
-
150
-
-
0036828143
-
Useful plants of dermatology. VI. The mayapple (Podophyllum)
-
Schwartz J., Norton S.A. Useful plants of dermatology. VI. The mayapple (Podophyllum). J. Am. Acad. Dermatol. 47:2002;774-775
-
(2002)
J. Am. Acad. Dermatol.
, vol.47
, pp. 774-775
-
-
Schwartz, J.1
Norton, S.A.2
-
151
-
-
0347926550
-
Biosynthesis of podophyllotoxin in Linum album cell cultures
-
Seidel V., Windhovel J., Eaton G., Alfermann A.W., Arroo R.R.J., Medarde M., Petersen M., Woolley J.G. Biosynthesis of podophyllotoxin in Linum album cell cultures. Planta. 215:2002;1031-1039
-
(2002)
Planta
, vol.215
, pp. 1031-1039
-
-
Seidel, V.1
Windhovel, J.2
Eaton, G.3
Alfermann, A.W.4
Arroo, R.R.J.5
Medarde, M.6
Petersen, M.7
Woolley, J.G.8
-
152
-
-
0035813468
-
Antitumor agents 210. Synthesis and evaluation of taxoid- epipodophyllotoxin conjugates as novel cytotoxic agents
-
Shi Q., Wang H.K., Bastow K.F., Tachibana Y., Chen K., Lee F.Y., Lee K.H. Antitumor agents 210. Synthesis and evaluation of taxoid-epipodophyllotoxin conjugates as novel cytotoxic agents. Bioorg. Med. Chem. 9:2001;2999-3004
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 2999-3004
-
-
Shi, Q.1
Wang, H.K.2
Bastow, K.F.3
Tachibana, Y.4
Chen, K.5
Lee, F.Y.6
Lee, K.H.7
-
153
-
-
0028835268
-
Topical treatment of genital warts in men, an open study of podophyllotoxin cream compared with solution
-
Strand A., Brinkeborn R.M., Siboulet A. Topical treatment of genital warts in men, an open study of podophyllotoxin cream compared with solution. Genitourin. Med. 71:1995;387-390
-
(1995)
Genitourin. Med.
, vol.71
, pp. 387-390
-
-
Strand, A.1
Brinkeborn, R.M.2
Siboulet, A.3
-
154
-
-
0032474530
-
Novel D-ring analogues of podophyllotoxin as potent anti-cancer agents
-
Subrahmanyam D., Renuka B., Rao C.V., Sagar P.S., Deevi D.S., Babu J.M., Vyas K. Novel D-ring analogues of podophyllotoxin as potent anti-cancer agents. Bioorg. Med. Chem. Lett. 8:1998;1391-1396
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1391-1396
-
-
Subrahmanyam, D.1
Renuka, B.2
Rao, C.V.3
Sagar, P.S.4
Deevi, D.S.5
Babu, J.M.6
Vyas, K.7
-
155
-
-
0033517015
-
9-deoxopodophyllotoxin derivatives as anti-cancer agents
-
Subrahmanyam D., Renuka B., Kumar G.S., Vandana V., Deevi D.S. 9-deoxopodophyllotoxin derivatives as anti-cancer agents. Bioorg. Med. Chem. Lett. 9:1999;2131-2134
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 2131-2134
-
-
Subrahmanyam, D.1
Renuka, B.2
Kumar, G.S.3
Vandana, V.4
Deevi, D.S.5
-
156
-
-
0031746653
-
Inhibitory effects of podophyllotoxin derivatives on herpes simplex virus replication
-
Sudo K., Konno K., Shigeta S., Yokota T. Inhibitory effects of podophyllotoxin derivatives on herpes simplex virus replication. Antivir. Chem. Chemother. 9:1998;263-267
-
(1998)
Antivir. Chem. Chemother.
, vol.9
, pp. 263-267
-
-
Sudo, K.1
Konno, K.2
Shigeta, S.3
Yokota, T.4
-
157
-
-
0141465298
-
Survey and enzymatic formation of lignans of Anthriscus sylvestris
-
Suzuki S., Sakakibara N., Umezawa T., Shimada M. Survey and enzymatic formation of lignans of Anthriscus sylvestris. J. Wood Sci. 48:2002;536-541
-
(2002)
J. Wood Sci.
, vol.48
, pp. 536-541
-
-
Suzuki, S.1
Sakakibara, N.2
Umezawa, T.3
Shimada, M.4
-
158
-
-
0028268623
-
Topical 0.3% and 0.5% podophyllotoxin cream for self-treatment of Molluscum contagiosum in males. A placebo-controlled, double-blind study
-
Syed T.A., Lundin S., Ahmad M. Topical 0.3% and 0.5% podophyllotoxin cream for self-treatment of Molluscum contagiosum in males. A placebo-controlled, double-blind study. Dermatology. 189:1994;65-68
-
(1994)
Dermatology
, vol.189
, pp. 65-68
-
-
Syed, T.A.1
Lundin, S.2
Ahmad, M.3
-
159
-
-
0029088624
-
Human leukocyte interferon-α versus podophyllotoxin in cream for the treatment of genital warts in males. A placebo-controlled, double-blind, comparative study
-
Syed T.A., Cheema K.M., Khayyami M., Ahmad S.A., Ahmad S.H., Ahmad S. Human leukocyte interferon-α versus podophyllotoxin in cream for the treatment of genital warts in males. A placebo-controlled, double-blind, comparative study. Dermatology. 191:1995;129-132
-
(1995)
Dermatology
, vol.191
, pp. 129-132
-
-
Syed, T.A.1
Cheema, K.M.2
Khayyami, M.3
Ahmad, S.A.4
Ahmad, S.H.5
Ahmad, S.6
-
160
-
-
0034073521
-
Characterization of human lung cancer cells resistant to 4′-O-demethyl-4β-(2″-nitro-4″-fluoroanilino) -4-desoxypodophyllotoxin, a unique compound in the epipodophyllotoxin antitumor class
-
Tachibana Y., Zhu X.K., Krishnan P., Lee K.H., Bastow K.F. Characterization of human lung cancer cells resistant to 4′-O-demethyl- 4β-(2″-nitro-4″-fluoroanilino)-4-desoxypodophyllotoxin, a unique compound in the epipodophyllotoxin antitumor class. Anticancer Drugs. 11:2000;19-28
-
(2000)
Anticancer Drugs
, vol.11
, pp. 19-28
-
-
Tachibana, Y.1
Zhu, X.K.2
Krishnan, P.3
Lee, K.H.4
Bastow, K.F.5
-
161
-
-
0032938486
-
Synthesis of novel 4β-1,2,3-triazol-1-yl) podophyllotoxins as potential antitumor drugs
-
Tao L., Wang Y.G., Ma C., Zheng B., Chen Y.Z. Synthesis of novel 4β-1,2,3-triazol-1-yl) podophyllotoxins as potential antitumor drugs. Synth. Commun. 29:1999;2053-2059
-
(1999)
Synth. Commun.
, vol.29
, pp. 2053-2059
-
-
Tao, L.1
Wang, Y.G.2
Ma, C.3
Zheng, B.4
Chen, Y.Z.5
-
162
-
-
0037136497
-
A multicomponent reaction for the one-pot synthesis of 4-aza-2,3-didehydropodophyllotoxin and derivatives
-
Tratrat C., Giorgi-Renault S., Husson H.P. A multicomponent reaction for the one-pot synthesis of 4-aza-2,3-didehydropodophyllotoxin and derivatives. Org. Lett. 4:2002;3187-3189
-
(2002)
Org. Lett.
, vol.4
, pp. 3187-3189
-
-
Tratrat, C.1
Giorgi-Renault, S.2
Husson, H.P.3
-
163
-
-
0021924089
-
Complement activating rheumatoid factors in rheumatoid arthritis studied by haemolysis in gel: Relation to antibody class and response to treatment with podophyllotoxin derivatives
-
Truedsson L., Sjoholm A.G., Stiurfelt G. Complement activating rheumatoid factors in rheumatoid arthritis studied by haemolysis in gel: relation to antibody class and response to treatment with podophyllotoxin derivatives. Clin. Exp. Rheumatol. 3:1985;29-37
-
(1985)
Clin. Exp. Rheumatol.
, vol.3
, pp. 29-37
-
-
Truedsson, L.1
Sjoholm, A.G.2
Stiurfelt, G.3
-
164
-
-
0037076856
-
Microtubule damaging agents induce apoptosis in HL 60 cells and G2/M cell cycle arrest in HT 29 cells
-
Tseng C.J., Wang Y.J., Liang Y.C., Jeng J.H., Lee W.S., Lin J.K., Chen C.H., Liu I.C., Ho Y.S. Microtubule damaging agents induce apoptosis in HL 60 cells and G2/M cell cycle arrest in HT 29 cells. Toxicology. 175:2002;123-142
-
(2002)
Toxicology
, vol.175
, pp. 123-142
-
-
Tseng, C.J.1
Wang, Y.J.2
Liang, Y.C.3
Jeng, J.H.4
Lee, W.S.5
Lin, J.K.6
Chen, C.H.7
Liu, I.C.8
Ho, Y.S.9
-
165
-
-
0032971496
-
Lignans from the seeds of Hernandia sonora
-
Udino L., Abaul J., Bourgeois P., Gorrichon L., Duran H., Zedde C. Lignans from the seeds of Hernandia sonora. Planta Med. 65:1999;279-281
-
(1999)
Planta Med.
, vol.65
, pp. 279-281
-
-
Udino, L.1
Abaul, J.2
Bourgeois, P.3
Gorrichon, L.4
Duran, H.5
Zedde, C.6
-
166
-
-
8944259912
-
Antitumor activity of a novel podophyllotoxin derivative (TOP-53) against lung cancer and lung metastatic cancer
-
Utsugi T., Shibata J., Sugimoto Y., Aoyagi K., Wierzba K., Kobunai T., Terada T., Oh-hara T., Tsuruo T., Yamada Y. Antitumor activity of a novel podophyllotoxin derivative (TOP-53) against lung cancer and lung metastatic cancer. Cancer Res. 56:1996;2809-2814
-
(1996)
Cancer Res.
, vol.56
, pp. 2809-2814
-
-
Utsugi, T.1
Shibata, J.2
Sugimoto, Y.3
Aoyagi, K.4
Wierzba, K.5
Kobunai, T.6
Terada, T.7
Oh-Hara, T.8
Tsuruo, T.9
Yamada, Y.10
-
167
-
-
0023810984
-
Effects of the ortho-quinone and catechol of the antitumor drug VP-16-213 on the biological activity of single-stranded and double-stranded phi X174 DNA
-
Van Maanen J.M.S., Lafleur M.V.M., Mans D.R.A., van den Akker E., de Ruiter C., Kootstra P.R., Pappie D., de Vries J., Retel J., Pinedo H.M. Effects of the ortho-quinone and catechol of the antitumor drug VP-16-213 on the biological activity of single-stranded and double-stranded phi X174 DNA. Biochem. Pharmacol. 37:1988;3579-3589
-
(1988)
Biochem. Pharmacol.
, vol.37
, pp. 3579-3589
-
-
Van Maanen, J.M.S.1
Lafleur, M.V.M.2
Mans, D.R.A.3
Van Den Akker, E.4
De Ruiter, C.5
Kootstra, P.R.6
Pappie, D.7
De Vries, J.8
Retel, J.9
Pinedo, H.M.10
-
168
-
-
34249961226
-
On the improvement of the podophyllotoxin production by phenylpropanoid precursor feeding to cell cultures of Podophyllum hexandrum Royle
-
Van Uden W., Pras N., Malingré T.M. On the improvement of the podophyllotoxin production by phenylpropanoid precursor feeding to cell cultures of Podophyllum hexandrum Royle. Plant Cell Tiss. Org. Cult. 23:1990;217-224
-
(1990)
Plant Cell Tiss. Org. Cult.
, vol.23
, pp. 217-224
-
-
Van Uden, W.1
Pras, N.2
Malingré, T.M.3
-
169
-
-
0028852795
-
The production of podophyllotoxin and its 5-methoxy derivative through bioconversion of cyclodextrin-complexed deoxypodophyllotoxin by plant cell cultures
-
Van Uden W., Bouma A.S., Bracht Waker J.F., Middel O., Wichers H.J., De Waard P., Woerdenbag H.J., Kellogg R.M., Pras N. The production of podophyllotoxin and its 5-methoxy derivative through bioconversion of cyclodextrin-complexed deoxypodophyllotoxin by plant cell cultures. Plant Cell Tiss. Org. Cult. 42:1995;73-79
-
(1995)
Plant Cell Tiss. Org. Cult.
, vol.42
, pp. 73-79
-
-
Van Uden, W.1
Bouma, A.S.2
Bracht Waker, J.F.3
Middel, O.4
Wichers, H.J.5
De Waard, P.6
Woerdenbag, H.J.7
Kellogg, R.M.8
Pras, N.9
-
170
-
-
0030933558
-
The large-scale isolation of deoxypodophyllotoxin from rhizomes of Anthriscus sylvestris followed by its bioconversion into 5- methoxypodophyllotoxin β-D-glucoside by cell cultures of Linun flavum
-
Van Uden W., Bos J.A., Boeke G.M., Woerdenbag H.J., Pras N. The large-scale isolation of deoxypodophyllotoxin from rhizomes of Anthriscus sylvestris followed by its bioconversion into 5-methoxypodophyllotoxin β-D-glucoside by cell cultures of Linun flavum. J. Nat. Prod.
-
(1997)
J. Nat. Prod.
, vol.60
, pp. 401-403
-
-
Van Uden, W.1
Bos, J.A.2
Boeke, G.M.3
Woerdenbag, H.J.4
Pras, N.5
-
171
-
-
0033583155
-
A high yield preparation of 2-fluoropodophyllotoxin
-
Van Vliet D.S., Lee K.H. A high yield preparation of 2- fluoropodophyllotoxin. Tetrahedron Lett. 40:1999;2259-2262
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 2259-2262
-
-
Van Vliet, D.S.1
Lee, K.H.2
-
172
-
-
0035953324
-
Antitumor agents. 207. Design, synthesis, and biological testing of 4β-anilino-2-fluoro-4′-demethylpodophyllotoxin analogues as cytotoxic and antiviral agents
-
Van Vliet D.S., Tachibana Y., Bastow K.F., Huang E.S., Lee K.H. Antitumor agents. 207. Design, synthesis, and biological testing of 4β-anilino-2- fluoro-4′-demethylpodophyllotoxin analogues as cytotoxic and antiviral agents. J. Med. Chem. 44:2001;1422-1428
-
(2001)
J. Med. Chem.
, vol.44
, pp. 1422-1428
-
-
Van Vliet, D.S.1
Tachibana, Y.2
Bastow, K.F.3
Huang, E.S.4
Lee, K.H.5
-
173
-
-
0010683104
-
Etoposide
-
D. Lednicer. Washington, DC: American Chemical Society
-
Von Wartburg A., Stähelin H. Etoposide. Lednicer D. Chronicles of Drug Discovery. 1993;349-380 American Chemical Society, Washington, DC
-
(1993)
Chronicles of Drug Discovery
, pp. 349-380
-
-
Von Wartburg, A.1
Stähelin, H.2
-
174
-
-
0027288674
-
Antitumor activity of a new low immunosuppressive derivative of podophyllotoxin (GP-11) and its mechanisms
-
Wang I.Z., Tian X., Tsumora H. Antitumor activity of a new low immunosuppressive derivative of podophyllotoxin (GP-11) and its mechanisms. Anticancer Drug Des. 8:1993;193-202
-
(1993)
Anticancer Drug Des.
, vol.8
, pp. 193-202
-
-
Wang, I.Z.1
Tian, X.2
Tsumora, H.3
-
175
-
-
0035216253
-
Preparation of new polymer from podophyllotoxin derivative
-
Wang J.Q., Zheng J., Cheng L., Li W.G., Su Z.X. Preparation of new polymer from podophyllotoxin derivative. Polym. Bull. 47:2001;223-230
-
(2001)
Polym. Bull.
, vol.47
, pp. 223-230
-
-
Wang, J.Q.1
Zheng, J.2
Cheng, L.3
Li, W.G.4
Su, Z.X.5
-
176
-
-
85044967919
-
Topical podophyllotoxin in psoriasis vulgaris
-
Wantke F., Flieschl G., Jarisch R. Topical podophyllotoxin in psoriasis vulgaris. Dermatology. 186:1993;79
-
(1993)
Dermatology
, vol.186
, pp. 79
-
-
Wantke, F.1
Flieschl, G.2
Jarisch, R.3
-
177
-
-
0027343731
-
Lignans, neolignans, and related compounds
-
Ward R.S. Lignans, neolignans, and related compounds. Nat. Prod. Rep. 10:1993;1-28
-
(1993)
Nat. Prod. Rep.
, vol.10
, pp. 1-28
-
-
Ward, R.S.1
-
178
-
-
0029278712
-
Lignans, neolignans, and related compounds
-
Ward R.S. Lignans, neolignans, and related compounds. Nat. Prod. Rep. 12:1995;183-205
-
(1995)
Nat. Prod. Rep.
, vol.12
, pp. 183-205
-
-
Ward, R.S.1
-
179
-
-
0030939744
-
Lignans, neolignans, and related compounds
-
Ward R.S. Lignans, neolignans, and related compounds. Nat. Prod. Rep. 14:1997;43-74
-
(1997)
Nat. Prod. Rep.
, vol.14
, pp. 43-74
-
-
Ward, R.S.1
-
180
-
-
0033083666
-
Lignans, neolignans and related compounds
-
Ward R.S. Lignans, neolignans and related compounds. Nat. Prod. Rep. 16:1999;75-96
-
(1999)
Nat. Prod. Rep.
, vol.16
, pp. 75-96
-
-
Ward, R.S.1
-
181
-
-
0035556440
-
The developmental ecology of mycorrhizal associations in mayapple, Podophyllum peltatum, Berberidaceae
-
Watson M.A., Scott K., Griffith J., Dieter S., Jones C.S., Nanda S. The developmental ecology of mycorrhizal associations in mayapple, Podophyllum peltatum, Berberidaceae. Evo. Ecol. 15:2001;425-442
-
(2001)
Evo. Ecol.
, vol.15
, pp. 425-442
-
-
Watson, M.A.1
Scott, K.2
Griffith, J.3
Dieter, S.4
Jones, C.S.5
Nanda, S.6
-
182
-
-
0001380216
-
Lignans and neolignans
-
Whiting D.A. Lignans and neolignans. Nat. Prod. Rep. 2:1985;191-211
-
(1985)
Nat. Prod. Rep.
, vol.2
, pp. 191-211
-
-
Whiting, D.A.1
-
183
-
-
0023424162
-
Lignans, neolignans, and related compounds
-
Whiting D.A. Lignans, neolignans, and related compounds. Nat. Prod. Rep. 4:1987;499-525
-
(1987)
Nat. Prod. Rep.
, vol.4
, pp. 499-525
-
-
Whiting, D.A.1
-
184
-
-
0011926265
-
Lignans, neolignans, and related compounds
-
Whiting D.A. Lignans, neolignans, and related compounds. Nat. Prod. Rep. 7:1990;349-364
-
(1990)
Nat. Prod. Rep.
, vol.7
, pp. 349-364
-
-
Whiting, D.A.1
-
185
-
-
0036213571
-
Treatment of genital warts - What's the evidence?
-
Wilson J. Treatment of genital warts - what's the evidence? Int. J. STD AIDS. 13:2002;216-222
-
(2002)
Int. J. STD AIDS
, vol.13
, pp. 216-222
-
-
Wilson, J.1
-
186
-
-
0037169983
-
Synthesis, hydrolytic activation and cytotoxicity of etoposide prodrugs
-
Wrasidlo W., Schröder U., Bernt K., Hübener N., Shabat D., Gaedicke G., Lode H. Synthesis, hydrolytic activation and cytotoxicity of etoposide prodrugs. Bioorg. Med. Chem. Lett. 12:2002;557-560
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 557-560
-
-
Wrasidlo, W.1
Schröder, U.2
Bernt, K.3
Hübener, N.4
Shabat, D.5
Gaedicke, G.6
Lode, H.7
-
187
-
-
0034736129
-
Dirigent-mediated podophyllotoxin biosynthesis in Linum flavum and Podophyllum peltatum
-
Xia Z.Q., Costa M.A., Proctor J., Davin L.B., Lewis N.G. Dirigent-mediated podophyllotoxin biosynthesis in Linum flavum and Podophyllum peltatum. Phytochemistry. 55:2000;537-549
-
(2000)
Phytochemistry
, vol.55
, pp. 537-549
-
-
Xia, Z.Q.1
Costa, M.A.2
Proctor, J.3
Davin, L.B.4
Lewis, N.G.5
-
188
-
-
0035918142
-
Secoisolariciresinol dehydrogenase purification, cloning, and functional expression - Implications for human health protection
-
Xia Z.Q., Costa M.A., Pelissier H.C., Davin L.B., Lewis N.G. Secoisolariciresinol dehydrogenase purification, cloning, and functional expression - implications for human health protection. J. Biol. Chem. 276:2001;12614-12623
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 12614-12623
-
-
Xia, Z.Q.1
Costa, M.A.2
Pelissier, H.C.3
Davin, L.B.4
Lewis, N.G.5
-
189
-
-
0036516128
-
Synthesis and insecticidal activity of novel 4α-halogenated benzoylamino podophyllotoxins against Pieris rapae Linnaeus
-
Xu H., Zhang X., Tian X., Lu M., Wang Y.G. Synthesis and insecticidal activity of novel 4α-halogenated benzoylamino podophyllotoxins against Pieris rapae Linnaeus. Chem. Pharm. Bull. 50:2002;399-402
-
(2002)
Chem. Pharm. Bull.
, vol.50
, pp. 399-402
-
-
Xu, H.1
Zhang, X.2
Tian, X.3
Lu, M.4
Wang, Y.G.5
-
190
-
-
0346355490
-
Two new methods for synthesis of 4β-amino-4-deoxypodophyllotoxin and 4β-amino-4′-demethyl-4-deoxypodophyllotoxin
-
You J.Z., Chen Y.Z. Two new methods for synthesis of 4β-amino-4- deoxypodophyllotoxin and 4β-amino-4′-demethyl-4-deoxypodophyllotoxin. Chem. J. Chin. 21:2000;1064-1066
-
(2000)
Chem. J. Chin.
, vol.21
, pp. 1064-1066
-
-
You, J.Z.1
Chen, Y.Z.2
-
191
-
-
0033525827
-
A facile and efficient synthesis of 4 β-aminopodophyllotoxins
-
Yu Y.P.C., Chen S.Y., Wang Y.G., Chen Y.Z. A facile and efficient synthesis of 4 β-aminopodophyllotoxins. Tetrahedron Lett. 40:1999;1967-1970
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 1967-1970
-
-
Yu, Y.P.C.1
Chen, S.Y.2
Wang, Y.G.3
Chen, Y.Z.4
-
193
-
-
4043052701
-
Synthesis and anti-cancer activity of novel derivatives of 4′-demethylepipodophyllotoxin
-
Zhang F.M., Tian X. Synthesis and anti-cancer activity of novel derivatives of 4′-demethylepipodophyllotoxin. Acta Chim. Sin. 60:2002;720-724
-
(2002)
Acta Chim. Sin.
, vol.60
, pp. 720-724
-
-
Zhang, F.M.1
Tian, X.2
-
196
-
-
0141974793
-
New lignan glycosides from chinese medicinal plant, Sinopodophillum emodi
-
Zhao C., Nagatsu A., Hatano K., Shirai N., Kato S., Ogihara Y. New lignan glycosides from chinese medicinal plant, Sinopodophillum emodi. Chem. Pharm. Bull. 51:2003;255-261
-
(2003)
Chem. Pharm. Bull.
, vol.51
, pp. 255-261
-
-
Zhao, C.1
Nagatsu, A.2
Hatano, K.3
Shirai, N.4
Kato, S.5
Ogihara, Y.6
-
197
-
-
0033168569
-
Antitumor agents. 194. Synthesis and biological evaluations of 4β-mono-, di-, and -trisubstituted aniline-4′-O-demethyl- podophyllotoxin and related compounds with improved pharmacological profiles
-
Zhu X.K., Guan J., Tachibana Y., Bastow K.F., Cho S.J., Cheng H.H., Cheng Y.C., Gurwith M., Lee K.H. Antitumor agents. 194. Synthesis and biological evaluations of 4β-mono-, di-, and -trisubstituted aniline-4′-O- demethyl-podophyllotoxin and related compounds with improved pharmacological profiles. J. Med. Chem. 42:1999;2441-2446
-
(1999)
J. Med. Chem.
, vol.42
, pp. 2441-2446
-
-
Zhu, X.K.1
Guan, J.2
Tachibana, Y.3
Bastow, K.F.4
Cho, S.J.5
Cheng, H.H.6
Cheng, Y.C.7
Gurwith, M.8
Lee, K.H.9
|